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Establishment of Patient-derived Orthotopic Xenografts (PDX) as Models for Pancreatic Ductal Adenocarcinoma.
Magouliotis, Dimitrios E; Lafazanis, Kostas; Koutsougianni, Fani; Sakellaridis, Nikos; Ioannou, Maria; Zacharoulis, Dimitris; Dimas, Konstantinos.
Afiliação
  • Magouliotis DE; Department of Cardiothoracic Surgery, University of Thessaly, Biopolis, Larissa, Greece.
  • Lafazanis K; Department of Pharmacology, University of Thessaly, Biopolis, Larissa, Greece.
  • Koutsougianni F; Department of Pharmacology, University of Thessaly, Biopolis, Larissa, Greece.
  • Sakellaridis N; Department of Pharmacology, University of Thessaly, Biopolis, Larissa, Greece.
  • Ioannou M; Department of Pathology, University of Thessaly, Biopolis, Larissa, Greece.
  • Zacharoulis D; Department of Surgery, University of Thessaly, Biopolis, Larissa, Greece.
  • Dimas K; Department of Pharmacology, University of Thessaly, Biopolis, Larissa, Greece; kdimas@uth.gr.
In Vivo ; 36(3): 1114-1119, 2022.
Article em En | MEDLINE | ID: mdl-35478141
BACKGROUND/AIM: Pancreatic cancer (PC) is one of the leading causes of cancer-related death. The purpose of the present study was to establish a patient-derived orthotopic xenograft model (PDOX) for pancreatic ductal adenocarcinoma (PDAC), thus providing a tumor microenvironment resembling that of the human pancreas to identify novel potential biomarkers and treatment regimens. MATERIALS AND METHODS: PDAC tissue samples were received from 35 patients, following informed consent, and three mouse strains were implemented. RESULTS: Successful PDOX engraftment was performed in nonobese diabetic/severe combined immunodeficient (NOD/SCID) and NOD/SCID gamma (NSG) mice. Nonetheless, we found a higher rate of successful engraftment and tumor growth in NSG compared to NOD/SCID mice, possibly owning to the different level of immunosuppression and more specifically of the natural killer cells presence. CONCLUSION: Our suggested PDOX model represents a preclinical cancer research model with a high affinity for the patient's tumor microenvironment, thus enabling the acceleration of PDAC research.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático Limite: Animals / Humans Idioma: En Revista: In Vivo Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Grécia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático Limite: Animals / Humans Idioma: En Revista: In Vivo Assunto da revista: NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Grécia